WO2007004553A1 - Procédé de production d’un condensateur à électrolyte solide - Google Patents

Procédé de production d’un condensateur à électrolyte solide Download PDF

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Publication number
WO2007004553A1
WO2007004553A1 PCT/JP2006/313087 JP2006313087W WO2007004553A1 WO 2007004553 A1 WO2007004553 A1 WO 2007004553A1 JP 2006313087 W JP2006313087 W JP 2006313087W WO 2007004553 A1 WO2007004553 A1 WO 2007004553A1
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WIPO (PCT)
Prior art keywords
solid electrolytic
electrolytic capacitor
semiconductor layer
producing
cathode
Prior art date
Application number
PCT/JP2006/313087
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English (en)
Japanese (ja)
Inventor
Kazumi Naito
Original Assignee
Showa Denko K. K.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Showa Denko K. K. filed Critical Showa Denko K. K.
Priority to EP06767695.7A priority Critical patent/EP1909298B1/fr
Priority to US11/994,393 priority patent/US8198126B2/en
Priority to JP2007524023A priority patent/JP5099831B2/ja
Publication of WO2007004553A1 publication Critical patent/WO2007004553A1/fr

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    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES OR LIGHT-SENSITIVE DEVICES, OF THE ELECTROLYTIC TYPE
    • H01G9/00Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
    • H01G9/0029Processes of manufacture
    • H01G9/0036Formation of the solid electrolyte layer
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES OR LIGHT-SENSITIVE DEVICES, OF THE ELECTROLYTIC TYPE
    • H01G9/00Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
    • H01G9/004Details
    • H01G9/022Electrolytes; Absorbents
    • H01G9/025Solid electrolytes
    • H01G9/028Organic semiconducting electrolytes, e.g. TCNQ
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES OR LIGHT-SENSITIVE DEVICES, OF THE ELECTROLYTIC TYPE
    • H01G9/00Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
    • H01G9/004Details
    • H01G9/04Electrodes or formation of dielectric layers thereon
    • H01G9/042Electrodes or formation of dielectric layers thereon characterised by the material
    • H01G9/0425Electrodes or formation of dielectric layers thereon characterised by the material specially adapted for cathode
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES OR LIGHT-SENSITIVE DEVICES, OF THE ELECTROLYTIC TYPE
    • H01G9/00Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
    • H01G9/004Details
    • H01G9/04Electrodes or formation of dielectric layers thereon
    • H01G9/048Electrodes or formation of dielectric layers thereon characterised by their structure
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES OR LIGHT-SENSITIVE DEVICES, OF THE ELECTROLYTIC TYPE
    • H01G9/00Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
    • H01G9/004Details
    • H01G9/04Electrodes or formation of dielectric layers thereon
    • H01G9/048Electrodes or formation of dielectric layers thereon characterised by their structure
    • H01G2009/05Electrodes or formation of dielectric layers thereon characterised by their structure consisting of tantalum, niobium, or sintered material; Combinations of such electrodes with solid semiconductive electrolytes, e.g. manganese dioxide
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES OR LIGHT-SENSITIVE DEVICES, OF THE ELECTROLYTIC TYPE
    • H01G9/00Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
    • H01G9/0029Processes of manufacture
    • H01G9/0032Processes of manufacture formation of the dielectric layer
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES OR LIGHT-SENSITIVE DEVICES, OF THE ELECTROLYTIC TYPE
    • H01G9/00Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
    • H01G9/15Solid electrolytic capacitors

Definitions

  • the present invention relates to a method for manufacturing a solid electrolytic capacitor in which a dielectric oxide film, a semiconductor layer, and an electrode layer are sequentially laminated on a sintered body of conductive powder and sealed with an exterior resin. More specifically, a solid electrolytic capacitor that can efficiently form a high-quality semiconductor layer on a dielectric oxide film of a sintered body that also has a conductive powder power, and that can produce a solid electrolytic capacitor with a good leakage current (LC). It relates to the manufacturing method. Background art
  • a solid electrolytic capacitor element in which a dielectric oxide film, a semiconductor layer, and an electrode layer are sequentially laminated on a sintered body of conductive powder is used as an exterior resin. There is a sealed solid electrolytic capacitor.
  • a solid electrolytic capacitor includes a sintered body of conductive powder such as tantalum having fine pores inside as one electrode (conductor), and a dielectric layer formed on a surface layer of the electrode and the dielectric It is manufactured by sealing a solid electrolytic capacitor element composed of the other electrode (usually a semiconductor layer) provided on the layer and the electrode layer laminated on the other electrode.
  • a solid electrolytic capacitor element composed of the other electrode (usually a semiconductor layer) provided on the layer and the electrode layer laminated on the other electrode.
  • the surface area inside the conductor increases as the pores become smaller and the amount of pores increases, so that the capacity of a capacitor made from the conductor increases.
  • a conductive polymer is exclusively used as an internal semiconductor layer.
  • Such a semiconductor layer is formed by chemical polymerization or electrolytic polymerization.
  • the semiconductor layer is formed by repeatedly immersing the conductor formed up to the dielectric layer alternately in a solution containing the oxidizer and dopant separately prepared except for the anode lead and a solution containing the monomer. It is formed.
  • the semiconductor layer is formed by a pure chemical reaction (solution reaction, gas phase reaction, and a combination thereof) without performing an energization operation, formed by an energization method, or a combination of these methods.
  • a pure chemical reaction solution reaction, gas phase reaction, and a combination thereof
  • an energization method for example, by energizing a cathode plate provided in a semiconductor layer forming solution with an electric conductor as an anode or an external electrode arranged in contact with or near the electric conductor as an anode.
  • a semiconductor layer is formed on the dielectric layer.
  • the constant current method is used to stably form a semiconductor layer when a semiconductor layer is formed by simultaneously energizing multiple conductors. It is preferable that
  • the cathode plate a stainless steel plate, a platinum plate, a tantalum plate, or the like, which is less corroded by the electric current solution, is used, for example, as described in Japanese Utility Model Publication No. 05-36267 (Patent Document 1).
  • An electric conductor group attached so as to protrude from the anode plate in a comb-like shape is immersed in a semiconductor layer forming tank, and a cathode plate is provided so as to face the anode plate.
  • a metal plate having electric field adjustment protrusions on the surface facing each conductor is used.
  • the surface area of conventional cathode metal plates, including this example has a microporous surface. The conductor has a smaller force than the total surface area of the group.
  • Patent Document 1 No. 05-36267
  • an object of the present invention is to efficiently form a high-quality semiconductor layer on a conductor having a dielectric oxide film on the surface when the semiconductor layer is formed by an energization operation using the conductor as an anode.
  • An object of the present invention is to provide a method for producing a solid electrolytic capacitor capable of producing a solid electrolytic capacitor having good LC.
  • the inventors of the present invention have formed a semiconductor when forming a semiconductor layer by an energization operation using a conductor having a dielectric oxide film on the surface as an anode.
  • a semiconductor when forming a semiconductor layer by an energization operation using a conductor having a dielectric oxide film on the surface as an anode.
  • the present invention provides the following method for producing a solid electrolytic capacitor and the method for producing the same.
  • the present invention relates to a manufactured solid electrolytic capacitor and its use.
  • a solid electrolytic capacitor in which a dielectric oxide film, a semiconductor layer, and an electrode layer are sequentially laminated on a sintered body of conductive powder to which an anode lead is connected, and sealed with an exterior resin.
  • a conductor layer having a dielectric oxide film is used as an anode and a semiconductor layer is formed on the dielectric oxide film by energizing a negative electrode provided in the electrolyte, the surface area is estimated to be 10% of the surface area.
  • a method for producing a solid electrolytic capacitor characterized by using a cathode more than doubled.
  • Conductor is a metal or alloy mainly composed of at least one selected from tantalum, niobium, titanium and aluminum, niobium oxide, or a mixture of at least two selected from these metals, alloys and niobium oxide. 2. The method for producing a solid electrolytic capacitor as described in 1 above.
  • the organic semiconductor is an organic semiconductor composed of benzopyrroline tetramer and chloranil, an organic semiconductor composed mainly of tetrathiotetracene, an organic semiconductor composed mainly of tetracyanoquinodimethane, the following general formula (1) or (2 )
  • R 1 ! ⁇ Each independently represents a hydrogen atom, an alkyl group having 1 to 6 carbon atoms or an alkoxy group having carbon atoms:! To 6; X represents an oxygen, iow or nitrogen atom; R 5 is present only when X is a nitrogen atom and represents a hydrogen atom or an alkyl group having from 6 to 6 carbon atoms, and R 1 and R 2 and R 3 and R 4 are bonded to each other to form a ring. Good.
  • a solid electrolytic capacitor as described in 7 above which is at least one kind selected from an organic semiconductor power mainly composed of a conductive polymer obtained by doping a polymer containing a repeating unit represented by a dopant with a dopant.
  • a conductive polymer containing a repeating unit represented by the general formula (1) is represented by the following general formula (3)
  • R ° and R ′ are each independently a hydrogen atom, a linear or branched saturated or unsaturated alkyl group having 1 to 6 carbon atoms, or the alkyl groups bonded to each other at an arbitrary position. And a substituent that forms a cyclic structure of at least one 5- to 7-membered saturated hydrocarbon containing two oxygen atoms, and the cyclic structure may be substituted.
  • Conductive polymer is polyalyrin, polyoxyphenylene, polyphenylene sulfide 9.
  • the semiconductor of conductivity is 10- 2 ⁇ : 10 3 S / cm range the solid electrolytic capacitor manufacturing method according to the 7 of.
  • the present invention relates to a method for producing a solid electrolytic capacitor in which a dielectric oxide film, a semiconductor layer, and an electrode layer are sequentially laminated on a sintered body of a conductor powder in which an anode lead is implanted, and sealed with an exterior resin.
  • a conductor having a dielectric oxide film on the surface is used as an anode and the semiconductor layer is formed on the dielectric oxide film by energizing between the cathode provided in the semiconductor layer forming solution, the surface area is increased.
  • the present invention provides a method for producing a solid electrolytic capacitor characterized by using a cathode having an apparent surface area of 10 times or more.
  • the apparent surface area is an area obtained from the external dimensions of the cathode and means an area in contact with the semiconductor layer forming solution. If the cathode is flat, its projected area (for example, vertical a If it is a rectangle of width b, it corresponds to a X b).
  • a high-quality semiconductor layer can be efficiently formed on a dielectric oxide film of a sintered body made of a conductive powder, and a solid electrolytic capacitor with good LC can be manufactured.
  • the sintered body used in the present invention is produced by sintering a powder compact of a conductor in which an anode lead is implanted on the surface of the compact.
  • the molding pressure for example, 0.1 to 50 kg / mm 2
  • the sintering conditions for example, temperature 800 to 1800 ° C ⁇ hour 1 minute to 10 hours
  • the surface area can be increased.
  • the surface of the sintered body may be chemically and / or electrically etched.
  • the shape of the sintered body is not particularly limited, and is usually a columnar shape. However, in the case of a prismatic shape, at least one of the corners is chamfered or spherically rounded and R is sintered.
  • the average value of the leakage current value (LC) of a solid electrolytic capacitor produced using a body may be kept good. Further, a taper may be provided so that the molded body can be easily detached from the mold during molding. In this case, the produced sintered body has a substantially truncated pyramid shape.
  • the conductor is selected from tantalum, aluminum, niobium, titanium, a force that is an alloy or niobium oxide mainly composed of these valve action metals, or the valve action metal, alloy, and conductive oxide. And a mixture of two or more.
  • At least one treatment selected from carbonization, phosphation, boronation, nitridation, sulfidation, and oxidation is performed on a part of the valve action metal, alloy or conductive compound, or the sintered body. It may be used after going.
  • the lead can be directly connected to the conductor. However, when the powdered conductor is formed or sintered after forming, a part of the lead prepared separately at the time of forming is used. It is also possible to form the lead together with the conductor and use the lead-out lead of the electrode on one side of the capacitor at a location outside the lead-out lead.
  • the anode lead may be linear, foil-shaped or plate-shaped. Further, the anode lead may be connected after the sintered body is produced without being implanted in the molded body.
  • As the material of the anode lead tantalum, aluminum, niobium, titanium, and alloys mainly composed of these valve action metals are used. Further, a part of the anode lead may be used after at least one treatment selected from carbonization, phosphide, boride, nitridation, sulfidation, and oxidation.
  • the strength of the sintered body can be maintained if the depth of the anode lead in the sintered body is 1/3 or more, preferably 2/3 or more of the sintered body. It is preferable because it can withstand the thermal and physical sealing stress when sealing the capacitor element, which will be described later.
  • insulation can be achieved by attaching an insulating resin in a headband shape to the boundary between the sintered body and the anode lead (on the anode lead side).
  • an insulating plate arranged through the anode lead may be provided.
  • a dielectric oxide film layer is formed on part of the surfaces of the sintered body and the anode lead.
  • metal oxide such as Ta ⁇ , Al ⁇ , TiO, NbO
  • the dielectric layer is a dielectric layer mainly composed of at least one selected from the above.
  • the anode substrate can be obtained by chemical conversion in an electrolytic solution. It may also be a dielectric layer in which a dielectric layer mainly composed of at least one selected from metal oxides and a dielectric layer used in a ceramic capacitor are mixed (WO 00/75943 pamphlet). (US6430026)).
  • Typical examples of the semiconductor layer formed on the dielectric layer in the present invention include at least one compound selected from an organic semiconductor and an organic semiconductor power.
  • organic semiconductors include organic semiconductors mainly composed of a conductive polymer obtained by doping a polymer containing a repeating unit represented by the following general formula (1) or (2) with a dopant.
  • I ⁇ to R 4 each independently represents a hydrogen atom, an alkyl group having 1 to 6 carbon atoms or an alkoxy group having 1 to 6 carbon atoms
  • X is Represents an oxygen atom, nitrogen atom, nitrogen atom
  • R 5 is present only when X is a nitrogen atom and represents a hydrogen atom or an alkyl group having 1 to 6 carbon atoms
  • R 1 and R 2 and R 3 and R 4 are They may be combined to form a ring.
  • the conductive polymer containing the repeating unit represented by the general formula (1) preferably includes a structural unit represented by the following general formula (3) as a repeating unit. Examples thereof include conductive polymers.
  • R 6 and R 7 are each independently a hydrogen atom, a straight-chain or branched saturated or unsaturated alkyl group having 16 carbon atoms, or the alkyl group at any position with respect to each other. And represents a substituent that forms a cyclic structure of at least one or more 5 7-membered saturated hydrocarbons containing two oxygen atoms.
  • the cyclic structure includes those having a vinylene bond which may be substituted and those having a phenyl structure which may be substituted.
  • a conductive polymer containing such a chemical structure is charged and doped with a dopant.
  • a dopant is not specifically limited, A well-known dopant can be used.
  • Examples of the polymer containing the repeating unit represented by the formulas (1) to (3) include polyaniline, polyoxyphenylene, polyphenylene sulfide, polythiophene, polyfuran, polypyrrole, polymethylbilol, And substituted derivatives and copolymers thereof. Of these, polypyrrole, polythiophene, and substituted derivatives thereof (for example, poly (3,4-ethylenedioxythiophene)) are preferred.
  • the inorganic semiconductor include at least one compound selected from molybdenum dioxide, tungsten dioxide, lead dioxide, manganese dioxide, and the like.
  • the ESR value of the manufactured capacitor is preferably reduced.
  • the semiconductor layer described above is formed by a pure chemical reaction (solution reaction, gas phase reaction, and a combination thereof) without performing an energization operation, formed by an energization method, or a combination of these methods.
  • the energization method is adopted at least once in the semiconductor layer forming step.
  • the conductor having a dielectric oxide film on the surface by an energization method is used as the anode.
  • a cathode having an apparent surface area of 10 times or more, preferably 30 times or more of the surface area is characterized by. This magnification is preferably as large as possible within the range that can be manufactured.
  • a plurality of (for example, 10 to 1000, preferably 10 to 200) anode parts of conductors are aligned and connected at equal intervals and on the long metal plate.
  • a metal frame in which a plurality of such long metal plates are arranged at equal intervals (for example, 10 to 500 sheets, preferably 10 to 200 sheets) is used as a conductor semiconductor forming portion on the metal frame. Then, it is placed so as to be immersed in a separately prepared solution for forming a semiconductor layer, and a semiconductor layer forming reaction is performed for a predetermined time.
  • a semiconductor layer is formed on the dielectric layer of the conductor by applying a predetermined constant DC current from the power supply terminal provided on the metallic frame toward the cathode plate provided in the semiconductor layer forming container.
  • the cathode plate provided in the semiconductor layer forming solution is used as an anti-cathode during energization, and an electrically conductive material, particularly a metal foil plate, is used.
  • the cathode plate a stainless plate, a tantalum plate, a platinum plate or the like is preferably used.
  • the surface area of the cathode plate is increased to more than 10 times the apparent surface area.
  • the method include a method using a platinum plate having platinum black formed on the surface as a cathode plate, a tantalum plate having platinum black attached to the surface, a niobium plate or a stainless steel plate.
  • a stainless steel plate, a tantalum plate, or a platinum plate for connecting a large number of conductors forming a semiconductor on the surface is connected by a welding method, and the surface area is increased by the connected conductor portions.
  • the semiconductor layer forming container itself is a cathode plate and a conductor is connected by welding is preferable.
  • the apparent surface area magnification is a value obtained by dividing the value measured by the BET method by the surface area of the original metal material surface.
  • Energization is performed using a plurality of cathode plates electrically connected to at least one feeding section.
  • a value obtained by dividing the standard deviation of the capacity of the manufactured capacitor group by the average value of the capacity is 10% or less, preferably 7% or less. More preferably, it can be made 5% or less.
  • the energization amount supplied to each conductor is determined by energizing with a predetermined constant current, but the remaining energization current value is constant even if the energization amount varies for some conductors for some reason. As a result, the current supply to each conductor is stabilized over the entire energization time.
  • the mass of the semiconductor layer is given by the integral value of the total current and time, so the capacitance of the capacitor proportional to the mass of the semiconductor layer stabilizes, and the standard deviation of the capacitance of the fabricated capacitor group Will be small.
  • the energization time and the predetermined current value vary depending on the type, size and density of the conductor used, the type and thickness of the formed dielectric layer, the type of semiconductor layer to be formed, and the like. Therefore, it is determined by a preliminary experiment.
  • As a method of preliminary experiments it is possible to judge the quality of a predetermined constant current value by managing the mass of the semiconductor layer. For example, there can be mentioned a method of plotting energization time and semiconductor mass at each constant current value in advance, and selecting the constant current value when the semiconductor mass that reaches the saturation value becomes the maximum.
  • the semiconductor layer forming solution includes a raw material that becomes a semiconductor when energized, and in some cases the aforementioned dopant (for example, aryl sulfonic acid or salt, alkyl sulfonic acid or salt, various polymer sulfonic acids or salts, and At least one known dopant such as a compound having each of the above-mentioned substituents is dissolved, and a semiconductor layer is formed on the dielectric layer by energization.
  • the temperature and ⁇ of the semiconductor layer forming solution are determined by preliminary experiments so that the semiconductor layer can be easily formed.
  • Re-chemical conversion can be performed in the same manner as the above-described method for forming a dielectric layer by chemical conversion.
  • the re-forming voltage is usually performed below the forming voltage.
  • an electrode layer is provided on the semiconductor layer formed by the above-described method or the like.
  • the electrode layer can be formed by, for example, solidification of a conductive paste, plating, metal deposition, adhesion of a heat-resistant conductive resin film, or the like.
  • a conductive paste for example, silver paste, copper paste, aluminum paste, carbon paste, nickel paste, etc. are preferred as the conductive paste. These may be used alone or in combination of two or more. When using 2 or more types, they may be mixed, or may be stacked as separate layers. After applying the conductive paste, leave it in the air or heat it to solidify.
  • the thickness of the conductive paste layer after solidification is usually about 0.1 to about 200 / im per layer.
  • the conductive paste usually contains 40 to 97% by mass of conductive powder. When the content is less than 40% by mass, the conductivity of the produced conductive paste is small. When the content exceeds 97% by mass, the adhesion of the conductive paste decreases. You may mix and use the conductive polymer and metal oxide powder which form the semiconductor layer mentioned above in the electrically conductive paste.
  • Examples of the plating include nickel plating, copper plating, silver plating, gold plating, and aluminum plating.
  • Examples of the deposited metal include aluminum, nickel, copper, silver, and gold.
  • an electrode layer is formed by sequentially laminating a carbon paste and a silver paste on a conductor on which a semiconductor layer is formed.
  • the capacitor element of the present invention having the above-described configuration is, for example, a resin mold, a resin case, or the like.
  • Capacitors for various applications can be made by using exteriors such as metal, metallic exterior cases, resin dating, and laminate film exteriors.
  • exteriors such as metal, metallic exterior cases, resin dating, and laminate film exteriors.
  • a chip-like capacitor having a resin mold exterior is particularly preferable because it can be easily reduced in size and cost.
  • resins used for sealing of solid electrolytic capacitors such as epoxy resin, phenol resin, alkyd resin, etc. can be adopted, but each resin is generally commercially available. It is preferable to use a low-stressed resin that can reduce the generation of sealing stress on the capacitor element that occurs at the time of sealing.
  • a transfer machine is preferably used as a manufacturing machine for sealing the resin. Preliminary experiments will be used to select the injection port for injecting the resin into the molding die installed in the transfer machine so as not to damage the capacitor element.
  • the capacitor thus fabricated may be subjected to an aging treatment in order to repair thermal and Z or physical deterioration of the dielectric layer when the electrode layer is formed or when it is packaged.
  • the aging method is performed by applying a predetermined voltage (usually within twice the rated voltage) to the capacitor. Aging time and temperature are determined in advance by experiment because optimum values vary depending on the type, capacity, and rated voltage of the capacitor. Normally, the time is several minutes and several days, and the temperature takes into account the thermal deterioration of the voltage application jig. It is performed at 300 ° C or below.
  • the atmosphere of aging can be air or a gas such as argon, nitrogen or helium.
  • a method for supplying water vapor is a method for supplying water vapor by heat in a water reservoir placed in an aging furnace.
  • the voltage application method can be designed to flow an arbitrary current such as a direct current, an alternating current having an arbitrary waveform, an alternating current superimposed on the direct current, or a pulse current. It is also possible to use a method in which the voltage is boosted at an arbitrary pattern up to a predetermined voltage. It is also possible to stop voltage application during aging and apply voltage again.
  • an arbitrary current such as a direct current, an alternating current having an arbitrary waveform, an alternating current superimposed on the direct current, or a pulse current. It is also possible to use a method in which the voltage is boosted at an arbitrary pattern up to a predetermined voltage. It is also possible to stop voltage application during aging and apply voltage again.
  • the capacitor manufactured in the present invention can be preferably used for a circuit that requires a high-capacity, low-LC capacitor, such as a central processing circuit and a power supply circuit. These circuits Can be used for various digital devices such as personal computers, servers, cameras, game consoles, DVDs, AV devices, mobile phones, and other electronic devices such as various power supplies. Since the capacitor manufactured according to the present invention has a high capacity and a good LC performance, an electronic circuit and an electronic device having a good performance can be obtained by using the capacitor.
  • the surface area of the cathode plate during the formation of the semiconductor layer used in the following examples and comparative examples was measured by the BET method (manufactured by Micrometritics, using Vacprep061).
  • CV 100,000 i F'V / g tantalum sintered body (size 4.5 X 3.3 X lmm, mass 81mg, lead wire 0.29mm ⁇ force S7mm exposed on the surface) was used as 640 conductors.
  • a polytetrafluoroethylene washer was attached to the lead wire to prevent the solution from splashing when the semiconductor layer was formed later.
  • the lead wires of the 32 sintered bodies were aligned and connected at equal intervals, leaving 30 mm on the left and right on a stainless steel long metal plate 250 mm long, 20 mm wide and 2 mm thick.
  • the metal frame is pulled up, washed with water, dried with alcohol, and dried, the metal frame is placed so that the sintered body and a part of the lead wire are immersed in the chemical conversion tank described above. Reforming (80 ° C, 30 minutes, 7V) was performed to repair defects in the current. After being pulled up and washed with water and dried, the energization and re-formation were repeated 12 times, followed by washing with water and washing with alcohol to form a semiconductor layer as a cathode. Next, a capacitor element in which a carbon paste tank, an acrylic resin 10 parts by mass, and a silver paste tank of 90 parts by mass of silver powder are successively immersed and dried to form a conductor layer and a cathode part. was made.
  • Example 3 In Example 1, except that the platinum plate affixed to the five surfaces of the semiconductor layer forming container was changed to a platinum plate with platinum black (Tsubakimura Metal Co., Ltd.) having a surface area of 110 times determined by the BET method. In the same manner as in Example 1, 640 solid electrolytic capacitors rated at 2.5 V were obtained. [0052]
  • Example 3 In Example 1, except that the platinum plate affixed to the five surfaces of the semiconductor layer forming container was changed to a platinum plate with platinum black (Tsubakimura Metal Co., Ltd.) having a surface area of 110 times determined by the BET method. In the same manner as in Example 1, 640 solid electrolytic capacitors rated at 2.5 V were obtained. [0052]
  • Example 3 Example 3:
  • Example 1 except that the platinum plate affixed to the five surfaces of the semiconductor layer forming container was a platinum plate with platinum black having a surface area determined by the BET method of 225 times (Kashimura Metal Co., Ltd.) In the same manner as in Example 1, 640 solid electrolytic capacitors rated at 2.5 V were obtained.
  • Example 1 a solid electrolytic capacitor was formed by forming a semiconductor layer in the same manner as in Example 1 except that a tantalum plate was attached as the cathode on the inner five surfaces of the semiconductor layer forming container, and conducting and re-forming were performed 12 times. 640 pieces were produced.
  • Example 1 a semiconductor layer was formed in the same manner as in Example 1 except that a tantalum plate was attached as the cathode to the inner five surfaces of the semiconductor layer formation container, and conduction and re-formation were performed 20 times. 640 capacitors were produced.
  • Example 1 the conductor is a CV 80,000 ⁇ F 'V / g niobium sintered body (the dimensions are the same as in Example 1. The mass is 54 mg), the formation voltage is 20 V, the dielectric layer is niobium pentoxide, constant. The current value is 18 mA (34 mA for the last two times), the number of times is 22 times, and the inner surface of the semiconductor layer forming vessel is scraped with platinum black from the surface of the same platinum plate used in Example 3 to obtain silver.
  • Example 6 640 solid electrolytic capacitors were fabricated in the same manner as in Example 1 except that the paste was pasted onto a tantalum plate, the cathode was 15 times the surface area of the projected area of the tantalum plate, and the re-forming voltage was set to 14 V and the rating was set to 4 V.
  • Example 1 the conductor was a CV 80,000 ⁇ F'VZg niobium sintered body, and in the same manner as in Example 4, platinum black was attached to the tantalum plate with a silver paste to make the surface area 55 times the surface area of the tantalum plate. In the same manner as in Example 4, 640 solid electrolytic capacitors were produced.
  • Example 1 the conductor was a CV 80,000 ⁇ F'VZg niobium sintered body, and platinum black was attached to the tantalum plate with silver paste in the same manner as in Example 4 to obtain a surface area 5 times the surface area of the tantalum plate. In the same manner as in Example 4, 640 solid electrolytic capacitors were produced. [0058] Comparative Example 3:
  • Example 4 640 solid electrolytic capacitors were prepared in the same manner as in Example 4 except that a tantalum plate was attached as the cathode to the inner 5 surfaces of the semiconductor layer forming container, and conduction and re-formation were performed 22 times. did.
  • Example 4 a semiconductor layer was formed in the same manner as in Example 4 except that a tantalum plate was attached as the cathode to the inner five surfaces of the semiconductor layer forming container, and conducting and re-forming were performed 30 times. 640 capacitors were produced.
  • Example 4 a stainless steel container with a length of 350 mm, a width of 170 mm, and a height of 45 mm was used as the semiconductor layer forming container, and 250 niobium sintered bodies equivalent to Example 4 were formed on the bottom surface and the inner surface of the four side. These lead wires were welded and connected, and a semiconductor layer was formed in the same manner as in Example 4 except that the negative electrode had a surface area 35 times the apparent surface area of the stainless steel plate, and 640 solid electrolytic capacitors were produced.
  • Capacitor capacity Measured at a room temperature of 120 Hz using an Hewlett Packard LCR measuring instrument.
  • Table 1 shows the measurement results.

Abstract

Procédé de production d’un condensateur à électrolyte solide par empilement séquentiel d’une pellicule d’oxyde diélectrique, d’une couche semi-conductrice et d’une couche d’électrode sur un corps fritté d’une poudre conductrice connectée à un connecteur puis par étanchéification de l’ouverture par une résine de revêtement. Lorsque la couche semi-conductrice est déposée sur la pellicule d’oxyde diélectrique par conduction entre une anode, c.-à-d. le conducteur comportant la pellicule d’oxyde diélectrique à sa surface, et une cathode présente dans un électrolyte, la couche semi-conductrice peut être obtenue efficacement au moyen d'une cathode dont l'aire de surface est supérieure ou égale à dix fois la surface apparente, ce qui permet de produire un condensateur à électrolyte solide présentant une bonne LC. La présente invention concerne également un condensateur produit par un tel procédé, et un circuit électronique et un dispositif utilisant un tel condensateur.
PCT/JP2006/313087 2005-06-30 2006-06-30 Procédé de production d’un condensateur à électrolyte solide WO2007004553A1 (fr)

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EP06767695.7A EP1909298B1 (fr) 2005-06-30 2006-06-30 Procédé de production d'un condensateur à électrolyte solide
US11/994,393 US8198126B2 (en) 2005-06-30 2006-06-30 Method for producing solid electrolytic capacitor
JP2007524023A JP5099831B2 (ja) 2005-06-30 2006-06-30 固体電解コンデンサの製造方法

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Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002246271A (ja) * 2001-02-16 2002-08-30 Matsushita Electric Ind Co Ltd 固体電解コンデンサの製造方法およびその製造装置
JP2003249420A (ja) * 2002-02-22 2003-09-05 Sanyo Electric Co Ltd 固体電解コンデンサの製造方法及び製造装置
JP2005167230A (ja) * 2003-11-13 2005-06-23 Showa Denko Kk 固体電解コンデンサ

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3254390A (en) * 1966-06-07 Electrolyte solution of
US4545883A (en) * 1982-07-19 1985-10-08 Energy Conversion Devices, Inc. Electrolytic cell cathode
DE3779870T2 (de) * 1986-11-08 1992-12-24 Showa Denko Kk Festelektrolytkondensator und verfahren zu seiner herstellung.
JPS63249323A (ja) * 1987-04-06 1988-10-17 松下電器産業株式会社 固体電解コンデンサ
JPH0536267Y2 (fr) 1988-02-12 1993-09-14
EP0372519B1 (fr) * 1988-12-07 1994-04-27 Matsushita Electric Industrial Co., Ltd. Condensateur à électrolyte solide
KR940007640B1 (ko) 1991-07-31 1994-08-22 삼성전자 주식회사 공통 입출력선을 가지는 데이타 전송회로
JPH05264499A (ja) 1992-03-19 1993-10-12 Nippon Steel Chem Co Ltd 酸化性物質濃度測定装置
US5469325A (en) * 1993-03-22 1995-11-21 Evans Findings Co. Capacitor
JP2586381B2 (ja) * 1993-07-05 1997-02-26 日本電気株式会社 固体電解コンデンサおよびその製造方法
JP2961491B2 (ja) 1994-04-27 1999-10-12 ケーデーケー株式会社 金属電極材料の作製方法
JP3776571B2 (ja) * 1997-09-18 2006-05-17 株式会社東芝 機能素子
US6375688B1 (en) * 1998-09-29 2002-04-23 Matsushita Electric Industrial Co., Ltd. Method of making solid electrolyte capacitor having high capacitance
TW479262B (en) * 1999-06-09 2002-03-11 Showa Denko Kk Electrode material for capacitor and capacitor using the same
JP3881480B2 (ja) * 1999-10-14 2007-02-14 ローム株式会社 固体電解コンデンサおよびその製法
JP3124272B1 (ja) * 1999-12-01 2001-01-15 花王株式会社 非水系二次電池

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002246271A (ja) * 2001-02-16 2002-08-30 Matsushita Electric Ind Co Ltd 固体電解コンデンサの製造方法およびその製造装置
JP2003249420A (ja) * 2002-02-22 2003-09-05 Sanyo Electric Co Ltd 固体電解コンデンサの製造方法及び製造装置
JP2005167230A (ja) * 2003-11-13 2005-06-23 Showa Denko Kk 固体電解コンデンサ

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JP5099831B2 (ja) 2012-12-19
US8198126B2 (en) 2012-06-12
JPWO2007004553A1 (ja) 2009-01-29
US20090086412A1 (en) 2009-04-02
EP1909298A4 (fr) 2015-07-29
EP1909298A1 (fr) 2008-04-09
EP1909298B1 (fr) 2019-05-08

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